The brain tissue response to implanted silicon microelectrode arrays is increased when the device is tethered to the skull

被引:257
作者
Biran, Roy
Martin, Dave C.
Tresco, Patrick A. [1 ]
机构
[1] Univ Utah, Coll Engn, Dept Bioengn, Keck Ctr Tissue Engn, Salt Lake City, UT 84112 USA
[2] Univ Michigan, Ctr Macromol Sci & Engn, Dept Mat Sci & Engn, Ann Arbor, MI 48109 USA
关键词
implant; silicon electrode; tissue response; foreign body response; neuroprosthetic;
D O I
10.1002/jbm.a.31138
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The influence of tethering silicon microelectrode arrays on the cortical brain tissue reaction was compared with that of untethered implants placed in the same location by identical means using immunoflourescent methods and cell type specific markers over indwelling periods of 1-4 weeks. Compared with untethered, freely floating implants, tethered microelectrodes elicited significantly greater reactivity to antibodies against ED1 and GFAP over time. Regardless of implantation method or indwelling time, retrieved microelectrodes contained a layer of attached macrophages identified by positive immunoreactivity against ED1. In the tethered condition and in cases where the tissue surrounding untethered implants had the highest levels of ED1+ and GFAP+ immunoreactivity, the neuronal markers for neurofilament 160 and NeuN were reduced. Although the precise mechanisms are unclear, the present study indicates that simply tethering silicon microelectrode arrays to the skull increases the cortical brain tissue response in the recording zone immediately surrounding the microelectrode array, which signals the importance of identifying this important variable when evaluating the tissue response of different device designs, and suggests that untethered or wireless devices may elicit less of a foreign body response. (c) 2007 Wiley Periodicals, Inc.
引用
收藏
页码:169 / 178
页数:10
相关论文
共 38 条
[11]  
Colton CA, 2000, ANN NY ACAD SCI, V899, P292
[12]   PERFORMANCE OF PLANAR MULTISITE MICROPROBES IN RECORDING EXTRACELLULAR SINGLE-UNIT INTRACORTICAL ACTIVITY [J].
DRAKE, KL ;
WISE, KD ;
FARRAYE, J ;
ANDERSON, DJ ;
BEMENT, SL .
IEEE TRANSACTIONS ON BIOMEDICAL ENGINEERING, 1988, 35 (09) :719-732
[13]   FACTORS INFLUENCING THE BIOCOMPATIBILITY OF INSERTABLE SILICON MICROSHAFTS IN CEREBRAL-CORTEX [J].
EDELL, DJ ;
TOI, VV ;
MCNEIL, VM ;
CLARK, LD .
IEEE TRANSACTIONS ON BIOMEDICAL ENGINEERING, 1992, 39 (06) :635-643
[14]  
EDGERTON BJ, 1982, ANN OTO RHINOL LARYN, V91, P117
[15]   Complement components of the innate immune system in health and disease in the CNS [J].
Gasque, P ;
Dean, YD ;
McGreal, EP ;
VanBeek, J ;
Morgan, BP .
IMMUNOPHARMACOLOGY, 2000, 49 (1-2) :171-186
[16]   Microglia as a source and target of cytokines [J].
Hanisch, UK .
GLIA, 2002, 40 (02) :140-155
[17]   Chronic response of adult rat brain tissue to implants anchored to the skull [J].
Kim, YT ;
Hitchcock, RW ;
Bridge, MJ ;
Tresco, PA .
BIOMATERIALS, 2004, 25 (12) :2229-2237
[19]   Role of nitric oxide in inflammation-mediated neurodegeneration [J].
Liu, B ;
Gao, HM ;
Wang, JY ;
Jeohn, GH ;
Cooper, CL ;
Hong, JS .
NITRIC OXIDE: NOVEL ACTIONS, DELETERIOUS EFFECTS AND CLINICAL POTENTIAL, 2002, 962 :318-331
[20]  
Liu X, 1999, IEEE Trans Rehabil Eng, V7, P315, DOI 10.1109/86.788468